🇺🇸 Daily vitamin D in United States

11 US adverse-event reports

Marketing authorisation

FDA

  • Status: approved

Safety signals — FAERS

Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.

Most-reported reactions

  1. Vomiting — 2 reports (18.18%)
  2. Abdominal Distension — 1 report (9.09%)
  3. Diarrhoea — 1 report (9.09%)
  4. Drug Intolerance — 1 report (9.09%)
  5. Eructation — 1 report (9.09%)
  6. Flatulence — 1 report (9.09%)
  7. Gastrointestinal Disorder — 1 report (9.09%)
  8. Headache — 1 report (9.09%)
  9. Illness — 1 report (9.09%)
  10. Nausea — 1 report (9.09%)

Source database →

Daily vitamin D in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is Daily vitamin D approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Daily vitamin D in United States?

Murdoch Childrens Research Institute is the originator. The local marketing authorisation holder may differ — check the official source linked above.